Attili Ilaria, Karachaliou Niki, Bonanno Laura, Berenguer Jordi, Bracht Jillian, Codony-Servat Jordi, Codony-Servat Carles, Ito Masaoki, Rosell Rafael
Department of Surgery, Oncology and Gastroenterology, University of Padova, Via Giustiniani 2, 53, Padova 35128, Italy.
Coyote Research Group, Pangaea Oncology, Laboratory of Molecular Biology, Quirón-Dexeus University Institute, Barcelona, Spain.
Ther Adv Med Oncol. 2018 Apr 2;10:1758835918763744. doi: 10.1177/1758835918763744. eCollection 2018.
Immune checkpoint blockade has modified the treatment landscape for many types of tumors, including lung cancer. Still our knowledge on the biology of the interaction between tumor cells and the microenvironment is limited, preventing the optimal use of these new compounds and the maximum benefit that the patients can derive from them. We have actively worked on the role of STAT3, a transcriptional factor that causes innate resistance to targeted therapies in oncogene-addicted tumors. In this short review we take the opportunity to express our opinion and review existing knowledge on the immune role of STAT3 and the possible implications that this may have for the discovery of new biomarkers to predict response to immunotherapy, as well as new partners to combine with and increase the efficacy of immune checkpoint inhibitors.
免疫检查点阻断已经改变了包括肺癌在内的多种肿瘤的治疗格局。然而,我们对肿瘤细胞与微环境之间相互作用的生物学知识仍然有限,这阻碍了这些新化合物的最佳应用以及患者从中获得的最大益处。我们积极研究了信号转导和转录激活因子3(STAT3)的作用,它是一种转录因子,在癌基因成瘾性肿瘤中导致对靶向治疗的固有抗性。在这篇简短的综述中,我们借此机会表达我们的观点,并回顾关于STAT3免疫作用的现有知识,以及这可能对发现预测免疫治疗反应的新生物标志物以及与免疫检查点抑制剂联合使用并提高其疗效的新伙伴的潜在影响。